| Tag | Content |
|---|
EnhancerAtlas ID | HS040-26988 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr4:6769480-6770690 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr4:6769942-6769957 | ACAGTCCAAAGTTCA | + | 6.64 | | SPIC | MA0687.1 | chr4:6770409-6770423 | CAAAAGAGGAAGGA | + | 6.03 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_09487 | chr4:6769697-6771025 | CD14 | | SE_23558 | chr4:6768960-6772695 | Colon_Crypt_1 | | SE_54218 | chr4:6769138-6770942 | Spleen |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I006767 | chr4 | 6769023 | 6776599 |
|
Enhancer Sequence | GGCCTGTCCC CCTGCCGCCC GCCCGGGCCA GGGAGATGGC CAATGCACGG CGGGCGCACC 60
CCTATTCCCT CCTCACTCAT GAGTCTGGTG GGACAACTCA TCCGGTCAGT CATGATGAGT 120
TGTCCCACTG CTGGGAACAC CTGCCCTGAG AGGTCTGGAT GGGCTCAGCC TCATGGCACC 180
AGAGCAGGCA GCTCGTGAGC AGCCCCGGGG GACCAGCAGG TCACTGGCAA CTGTTAAGCT 240
GTGGAGAACT TCTCAGGGCT CAGCTGGCAT TCCGACCTCC CTTTGCCTCC CACGGGCCTG 300
GGCGGGGCCC CTTCCTTTCG TCCTTAGCCA GCCGCCACTC TGTCCTCCAC TGGGAGTCCC 360
TGCCCCCATT ACTGCACCAG CTCCCCTCCC CCCACCCTGA GGACACCCAC CCTGTTCGTT 420
ATAAAGGGAC ACAGGCACAG CTAACAAGGA ACAATTGTGG GCACAGTCCA AAGTTCAGGG 480
TTTTAAGGAC ACCGTTTCCG CCCCGGCCTC GTCTCTGAGA TGATTCTGGG CCCATCAGAG 540
GCTTCCGGCT TCTCCTTTTA TGACCCTGAG CTTGTCGGTC TCCCTATCCT CATGCCCCCT 600
GCCCTTGGAG AGACCCAGCC TTCCTTCTAC AAGATCCCCT GCTGAGGGAG AAGGAGCTGG 660
CTGGGGCAGG ACCGTAGGCT CAGGCTACAT GCCCCAAGTT CACTCTCAGC TCACATGCTC 720
CAGACATTGT CCTGGTGCTC AGCCTGCCAT CCAGGAGGCC CCTCCCAAGC TCCTGGGCTT 780
CCATCCTCAG TGATCCAGTG GACCTGGTTC CCAGAGCTGG GTGGGAAAGG GCCCCTTGCC 840
TCTGGGATGG GAGGAAAATG TTCAGTCCTC TGTTAAGCTG GTCGCAGACT CTGATGAACC 900
TTTCCAGGGC CATGAGTCAT GCCGTTTTCC AAAAGAGGAA GGAGGCTCGG GGAGAGTAAG 960
TGTCTTGCCC AAAGTCACAC AGTGGAGTCA GCACTTGAAT TTAGCTCTGA CTCCCATGGC 1020
ACCTGCTGAG TGCCTGACCT GCCCCCTCCA TCCCCCATGG CCTGCCTGCT CCTCGGTGCA 1080
AGGATCACCT CAGCTGTCAC AGCTTTAGAA GTGAGCTGTG CATGAACCCC TGAACCCCAA 1140
AGCATCAGGG AGGGTCACCC AGAACCCCAT GCCTGCTGGA TGCCGAAGCC ATGCCAAATA 1200
AATGGGACAG 1210
|
